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Disease Ontology Browser
dentatorubral-pallidoluysian atrophy (DOID:0060162)
Alliance: disease page
Synonyms: DRPLA; Haw River Syndrome; Naito-Oyanagi disease
Alt IDs: OMIM:125370, MESH:D020191, NCI:C122653, UMLS_CUI:C0751781
Definition: An autosomal dominant cerebellar ataxia that has_material_basis_in expansion of CAG triplet repeats (glutamine) encoding a polyglutamine tract in the atrophin-1 protein.

Disease References using Mouse Models (3)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory